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Services for Pharmaceutical Packaging Materials


TÜV Rheinland

In the pharmaceutical industry, it is not only the medicine or medical device that counts, but how it is packaged as well. Safe, sanitary packaging is essential and requires careful design and assembly. To ensure that your pharmaceuticals are wrapped and boxed in accordance with regulations and consumer expectations, as well as your company’s own standards of excellence, you can rely on our services for pharmaceutical packaging materials. Our experts can accompany you through every phase of packaging development and production with an eye to optimal safety and international compliance.

Medical Device Safety and Testing at a Glance

Medical Device Regulation (MDR) 2017/745

Start here. - Check the newest regulations, certificate transition dates, and common FAQs for in vitro diagnostic and medical device requirements. Are you prepared for EU, US and key market approval?

New Regulations for Medical Products

pdf New IVDR 1 MB Download
pdf MDR / IVDR declaration of interest 92 KB Download
pdf Regulation (EU) 2017/745 1 MB Download
pdf Regulation (EU) 2020/561 522 KB Download

Our portfolio

Artificial Intelligence for Products
Artificial Intelligence for Products 

A guide for understanding the impacts of the EU AI ACT on Products

Tested Medical Device
Non-Active Medical Device Testing 

Increase your competitive edge and certify your non-active medical device products.

ISO 15378 Certification
ISO 15378 Certification 

We conduct ISO 15378 quality management system (QMS) compliance validation for suppliers of primary packaging for pharmaceutical and medicinal products.

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Get in contact with us!

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